← Back to catalogue

Lumitex 4mm Universal Fiber Optic Cable

FDA UDI

Class I (US FDA UDI)

by Lumitex, Inc.

Identity

Trade Name
Lumitex 4mm Universal Fiber Optic Cable FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Model / Reference
012139 FDA UDI

Identifiers

Catalog Number
012681 FDA UDI
Primary DI / UDI-DI
00812432021689 FDA UDI
FDA Product Code
FDG FDA UDI
GMDN Term
Fibreoptic light cable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4530 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fibreoptic light cable

Lumitex 4mm Universal Fiber Optic Cable by Lumitex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic light cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Lumitex, Inc.

Sources (1)

  • FDA UDI 75d847a2-50e5-4c3f-95c9-c3439e53c6e1 33 fields · synced May 30, 2026